TSN | |||||||||||||||||||||||||||||||||||||||||||||||||||
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Aliases | TSN , BCLF-1, C3PO, RCHF1, REHF-1, TBRBP, TRSLN, translin | ||||||||||||||||||||||||||||||||||||||||||||||||||
External IDs | OMIM: 600575 MGI: 109263 HomoloGene: 3397 GeneCards: TSN | ||||||||||||||||||||||||||||||||||||||||||||||||||
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Wikidata | |||||||||||||||||||||||||||||||||||||||||||||||||||
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Translin is a DNA-binding protein that in humans is encoded by the TSN gene. [5] [6] [7] Together with translin-associated factor X, translin forms the component 3 of promoter of RISC (C3PO) complex which facilitates endonucleolytic cleavage of the passenger strand during microRNA loading into the RNA-induced silencing complex (RISC). [8] [9] [10]
This gene encodes a DNA-binding protein which specifically recognizes conserved target sequences at the breakpoint junction of chromosomal translocations. Translin polypeptides form a multimeric structure that is responsible for its DNA-binding activity. Recombination-associated motifs and translin-binding sites are present at recombination hotspots and may serve as indicators of breakpoints in genes which are fused by translocations. These binding activities may play a crucial role in chromosomal translocation in lymphoid neoplasms. [7]
High-mobility group AT-hook 2, also known as HMGA2, is a protein that, in humans, is encoded by the HMGA2 gene.
Cyclic AMP-dependent transcription factor ATF-1 is a protein that in humans is encoded by the ATF1 gene.
4F2 cell-surface antigen heavy chain is a protein that in humans is encoded by the SLC3A2 gene.
RNA-binding protein EWS is a protein that in humans is encoded by the EWSR1 gene on human chromosome 22, specifically 22q12.2. It is one of 3 proteins in the FET protein family. The q22.2 region of chromosome 22 encodes the N-terminal transactivation domain of the EWS protein and that region may become joined to one of several other chromosomes which encode various transcription factors, see and the FET protein family. The expression of a chimeric protein with the EWS transactivation domain fused to the DNA binding region of a transcription factor generates a powerful oncogenic protein causing Ewing sarcoma and other members of the Ewing family of tumors. These translocations can occur due to chromoplexy, a burst of complex chromosomal rearrangements seen in cancer cells. The normal EWS gene encodes an RNA binding protein closely related to FUS (gene) and TAF15, all of which have been associated to amyotrophic lateral sclerosis.
Protein SET, also known as Protein SET 1, is a protein that in humans is encoded by the SET gene.
RAD52 homolog , also known as RAD52, is a protein which in humans is encoded by the RAD52 gene.
Protein SSX2 is a protein that in humans is encoded by the SSX2 gene.
Hepatic leukemia factor is a protein that in humans is encoded by the HLF gene.
Lysine-specific demethylase 5A is an enzyme that in humans is encoded by the KDM5A gene.
60S ribosomal protein L22 is a protein that in humans is encoded by the RPL22 gene on Chromosome 1.
Translin-associated protein X is a protein that in humans is encoded by the TSNAX gene.
Protein lyl-1 is a protein that in humans is encoded by the LYL1 gene.
Zinc finger protein 238 is a zinc finger containing transcription factor that in humans is encoded by the ZNF238 gene.
Putative RNA-binding protein 15 is a protein that in humans is encoded by the RBM15 gene. It is an RNA-binding protein that acts as a key regulator of N6-Methyladenosine (m6A) methylation of RNAs
45 kDa calcium-binding protein is a protein that in humans is encoded by the SDF4 gene.
Coatomer subunit zeta-1 is a protein that in humans is encoded by the COPZ1 gene.
Zinc finger protein 346 is a protein that in humans is encoded by the ZNF346 gene.
Iron-sulfur cluster assembly 1 homolog, mitochondrial is an evolutionarily highly conserved protein for the biogenesis of iron-sulfur cluster across species. In humans it is encoded by the ISCA1 gene.
ATP-binding cassette sub-family B member 8, mitochondrial is a protein that in humans is encoded by the ABCB8 gene.
PR domain zinc finger protein 9 is a protein that in humans is encoded by the PRDM9 gene. PRDM9 is responsible for positioning recombination hotspots during meiosis by binding a DNA sequence motif encoded in its zinc finger domain. PRDM9 is the only speciation gene found so far in mammals, and is one of the fastest evolving genes in the genome.